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Hepatitis Concerns Emerge after Lockdowns, SARS-CoV-2, and Mass Vaccination
We were made aware of reports from Bril and Boettler in the medical literature that forms of autoimmune hepatitis were emerging after the COVID-19 vaccination.1,2 This was on the heels of a report from Alden and colleagues that discovered reverse transcription of the Pfizer–BioNTech COVID-19 vaccine mRNA code into liver cell DNA.3
This created the possibility that some hepatocytes may harbor the genetic code for the Wuhan wild-type Spike protein and, thus, may be primed for liver injury with a superimposed hepatic insult or infection. Lensen et al. have now reported fatal hepatitis C reactivation after COVID-19 vaccination with Pfizer–BioNTech COVID-19 vaccine.4
Reports are summarized in this issue of the McCullough Report about a breaking series of cases of adenoviral hepatitis in children, with several requiring liver transplantation. This raises the concern that the history of COVID-19 vaccination is not being presented or considered in these cases. It should be clear that when serious medical problems arise, in each and every case, there must be accounting for both the SARS-CoV-2 respiratory infection as well as COVID-19 vaccination in the case record.
Both give exposure to the Spike protein, which is known to be injurious to every cell line that it touches. Additionally, the Spike protein damages the endothelial cells that line blood vessels, and it directly causes blood clotting even in the absence of platelets, and thus blood vessel injury and clotting, which is common to many acute organ injury syndromes, should be considered a complication of SARS-CoV-2 infection and or COVID-19 vaccination until proven otherwise.5
We have a great show for you this week, including exclusive interviews done on the road in the panhandle of Florida with Dr. Carrie Madej, who gives us consideration of the future concerning transhumanism, faith, and our spiritual resolve to endure what is happening all around us.
Finally, we bring to the microphone for the first time on the McCullough Report, Dr. Ryan Cole, who is a world-leading expert on clinical and anatomic pathology and what we have learned from SARS-CoV-2 infection as well as the wide array of injuries that we are witnessing from COVID-19 vaccination.
Our music segment upfront in the program is “Let the World Go Free” by Joseph Langham.
So let’s get real, let’s get loud; on America Out Loud Talk Radio, this is The McCullough Report!
The McCullough Report: Sat/Sun 2 PM ET Encore 7 PM – Internationally recognized Dr. Peter A. McCullough, known for his iconic views on the state of medical truth in America and around the globe, pierces through the thin veil of mainstream media stories that skirt the significant issues and provide no tractable basis for durable insight. Listen on iHeart Radio, our world-class media player, or our free apps on Apple, Android, or Alexa. Each episode goes to major podcast networks early in the week and can be heard on-demand anywhere in the world.
1 Bril F, Al Diffalha S, Dean M, Fettig DM. Autoimmune hepatitis developing after coronavirus disease 2019 (COVID-19) vaccine: Causality or casualty? J Hepatol. 2021 Jul;75(1):222-224. doi: 10.1016/j.jhep.2021.04.003. Epub 2021 Apr 20. PMID: 33862041; PMCID: PMC8056822.
2 Boettler T, Csernalabics B, Salié H, Luxenburger H, Wischer L, Alizei ES, Zoldan K, Krimmel L, Bronsert P, Schwabenland M, Prinz M, Mogler C, Neumann-Haefelin C, Thimme R, Hofmann M, Bengsch B. SARS-CoV-2 vaccination can elicit a CD8 T-cell dominant hepatitis. J Hepatol. 2022 Apr 21:S0168-8278(22)00234-3. doi: 10.1016/j.jhep.2022.03.040. Epub ahead of print. PMID: 35461912.
3 Aldén M, Olofsson Falla F, Yang D, Barghouth M, Luan C, Rasmussen M, De Marinis Y. Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line. Current Issues in Molecular Biology. 2022; 44(3):1115-1126. https://doi.org/10.3390/cimb44030073
5 Zhang J, Tecson KM, McCullough PA. Role of endothelial cell receptors in the context of SARS-CoV-2 infection (COVID-19). Proc (Bayl Univ Med Cent). 2021 Jan 26;34(2):262-268. doi: 10.1080/08998280.2021.1874231. PMID: 33664552; PMCID: PMC7852287.
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